Canonical Allele Identifier: CA364457927

Gene: EFHC1

Linked Data

• MyVariant Identifiers: chr6:g.52344472C>G (hg19) ; chr6:g.52479674C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479674C>G , CM000668.2:g.52479674C>G	GRCh38
NC_000006.11:g.52344472C>G , CM000668.1:g.52344472C>G	GRCh37
NC_000006.10:g.52452431C>G	NCBI36
NG_016760.1:g.64479C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1527C>G MANE Select	ENSP00000360107.4:p.Asp509Glu
ENST00000480623.6:c.1527C>G	ENSP00000434498.2:p.Asp509Glu
ENST00000635760.1:c.1203C>G	ENSP00000489765.1:p.Asp401Glu
ENST00000635812.1:c.*828C>G	ENSP00000490859.1:n.*828C>G
ENST00000635866.1:c.*1396C>G	ENSP00000489866.1:n.*1396C>G
ENST00000635911.1:n.3045C>G
ENST00000635984.1:c.1203C>G	ENSP00000489921.1:p.Asp401Glu
ENST00000635996.1:c.1527C>G	ENSP00000490256.1:p.Asp509Glu
ENST00000636107.1:c.1527C>G	ENSP00000489680.1:p.Asp509Glu
ENST00000636311.1:n.1421C>G
ENST00000636343.1:c.1193C>G
ENST00000636379.1:c.1239C>G	ENSP00000490622.1:p.Asp413Glu
ENST00000636398.1:c.1227C>G	ENSP00000489654.1:n.1227C>G
ENST00000636489.1:c.1470C>G	ENSP00000489998.1:p.Asp490Glu
ENST00000636616.1:n.1088C>G
ENST00000636702.1:c.1497C>G	ENSP00000489623.1:p.Asp499Glu
ENST00000636954.1:c.1470C>G	ENSP00000489966.1:p.Asp490Glu
ENST00000637089.1:c.1527C>G	ENSP00000489854.1:p.Asp509Glu
ENST00000637121.1:n.1329C>G
ENST00000637263.1:c.1527C>G	ENSP00000489700.1:p.Asp509Glu
ENST00000637340.1:n.3452C>G
ENST00000637353.1:c.1527C>G	ENSP00000490441.1:p.Asp509Glu
ENST00000637602.1:c.*1228C>G	ENSP00000490074.1:n.*1228C>G
ENST00000637849.1:n.1591C>G
ENST00000637874.1:c.472C>G	ENSP00000490348.1:n.472C>G
ENST00000637892.1:n.1731C>G
ENST00000371068.9:c.1527C>G	ENSP00000360107.4:p.Asp509Glu
ENST00000480623.5:c.*1947C>G	ENSP00000434498.1:n.*1947C>G
ENST00000538167.2:c.1470C>G	ENSP00000444521.1:p.Asp490Glu
NM_001172420.1:c.1470C>G	NP_001165891.1:p.Asp490Glu
NM_018100.3:c.1527C>G	NP_060570.2:p.Asp509Glu
NR_033327.1:n.2999C>G
NM_018100.4:c.1527C>G MANE Select	NP_060570.2:p.Asp509Glu
NM_001172420.2:c.1470C>G	NP_001165891.1:p.Asp490Glu
NR_033327.2:n.2853C>G